INT347220

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Context Info
Confidence 0.49
First Reported 2008
Last Reported 2008
Negated 0
Speculated 1
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 0.28
Pain Relevance 0

This is a graph with borders and nodes. Maybe there is an Imagemap used so the nodes may be linking to some Pages.

extracellular region (Serpina3c)
Serpina3c (Mus musculus)
Pain Link Frequency Relevance Heat
Potency 3 5.00 Very Low Very Low Very Low
headache 2 5.00 Very Low Very Low Very Low
pruritus 1 5.00 Very Low Very Low Very Low
cytokine 1 5.00 Very Low Very Low Very Low
Pain 1 5.00 Very Low Very Low Very Low
backache 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Hyperbilirubinemia 2 98.26 Very High Very High Very High
Gilbert Syndrome 1 96.72 Very High Very High Very High
Congenital Anomalies 3 88.24 High High
Chronic Myeloid Leukemia 3 50.00 Quite Low
Pleural Effusion 1 49.12 Quite Low
Death 1 35.72 Quite Low
Thrombocytopenia 6 9.76 Low Low
Myeloid Leukemia 39 5.00 Very Low Very Low Very Low
Leukemia 14 5.00 Very Low Very Low Very Low
Philadelphia Chromosome 12 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
The etiology of hyperbilirubinemia was explored in 62 patients by examining the polymorphisms in the uridine diphosphate glucurosyltransferase 1A1 (UGT1A1) gene: the results indicated that the repeat of TA, which predisposes to Gilbert syndrome, predicted for susceptibility to side effect under nilotinib.
Spec (examining) Positive_regulation (glucurosyltransferase) of Gene_expression (glucurosyltransferase) of 1A1 associated with gilbert syndrome and hyperbilirubinemia
1) Confidence 0.49 Published 2008 Journal OncoTargets and therapy Section Body Doc Link PMC2994207 Disease Relevance 0.28 Pain Relevance 0

General Comments

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